Home > National Drug Code (NDC) > Cetirizine Hydrochloride

Cetirizine Hydrochloride - 0536-4088-11 - (Cetirizine)

Alphabetical Index


Drug Information of Cetirizine Hydrochloride

Product NDC: 0536-4088
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 0536-4088
Labeler Name: Rugby Laboratories Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078780
Marketing Category: ANDA
Start Marketing Date: 20120323

Package Information of Cetirizine Hydrochloride

Package NDC: 0536-4088-11
Package Description: 4 BLISTER PACK in 1 BOX (0536-4088-11) > 90 TABLET in 1 BLISTER PACK

NDC Information of Cetirizine Hydrochloride

NDC Code 0536-4088-11
Proprietary Name Cetirizine Hydrochloride
Package Description 4 BLISTER PACK in 1 BOX (0536-4088-11) > 90 TABLET in 1 BLISTER PACK
Product NDC 0536-4088
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120323
Marketing Category Name ANDA
Labeler Name Rugby Laboratories Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


General Information